Canonical Allele Identifier: PA2826454978
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1449
ClinVar RCV Id: RCV000001514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245138.1:p.Arg132Gln
CA251802
NM_001258209.2:c.395G>A